Nisha M Nair, Lucas Mendicino, Peter N Fiorica, Angela R Omilian, Thaer Khoury, Wiam Bshara, Elisa V Bandera, Chi-Chen Hong, Yara Abdou, Jo L Freudenheim, Anselm J M Hennis, Katie M O'Brien, Gary R Zirpoli, Ebonee N Butler, John Oladapo Obafunwa, Clarice R Weinberg, Dezheng Huo, Bingshan Li, Xingyi Guo, Julie R Palmer, Christopher A Haiman, Wei Zheng, Song Yao, Christine B Ambrosone
{"title":"达菲抗原趋化因子受体(DARC)基因的非洲特异性变异、CD8+ t细胞密度和黑人女性侵袭性乳腺癌亚型","authors":"Nisha M Nair, Lucas Mendicino, Peter N Fiorica, Angela R Omilian, Thaer Khoury, Wiam Bshara, Elisa V Bandera, Chi-Chen Hong, Yara Abdou, Jo L Freudenheim, Anselm J M Hennis, Katie M O'Brien, Gary R Zirpoli, Ebonee N Butler, John Oladapo Obafunwa, Clarice R Weinberg, Dezheng Huo, Bingshan Li, Xingyi Guo, Julie R Palmer, Christopher A Haiman, Wei Zheng, Song Yao, Christine B Ambrosone","doi":"10.1158/1055-9965.EPI-25-0454","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Immune response in blood varies by ancestry, linked to an African-specific variant (rs2814778) in DARC/ACKR1. We examined associations between rs2814778, CD8+ T cell density in breast tumors, and breast cancer risk in African-American/Black women.</p><p><strong>Methods: </strong>CD8+ T-cell density in tumors from 428 Black women were examined in relation to the rs2814778 variant. In the African Ancestry Breast Cancer Genetics Consortium (AABCG) with 16,886 cases and 18,044 controls, rs2814778 was evaluated in relation to risk of overall breast cancer and to more aggressive subtypes (ER- and TNBC).</p><p><strong>Results: </strong>Women with the African-specific CC genotype had lower tumor CD8+ T-cell density (87.0 per mm2) than those with TT genotypes (146.6 per mm2; p< 0.05). Each T allele was significantly associated with an increase in T-cell density (p=0.04). In the largest analysis, to date, there were no associations between rs2814778 and risk of overall breast cancer [OR=0.90 (95% CI 0.66-1.22)], or with ER- [OR=0.86 (95% CI 0.68-1.08)] or TNBC [OR=0.77 (95% CI 0.56-1.05)].</p><p><strong>Conclusions: </strong>Although breast tumors from women with the African-specific DARC C allele had lower CD8+ T-cell density levels than those with T alleles, in a large breast cancer consortium with adequate statistical power, the variant was not associated with breast cancer risk overall, nor with risk of ER- or TNBC as previously hypothesized.</p><p><strong>Impact: </strong>Although the 'Duffy-null' allele has been the focus of research as a contributor to aggressive breast cancer in Black women, this study with 34,930 cases and controls found no associations with risk.</p>","PeriodicalId":520580,"journal":{"name":"Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The African-specific variant in the Duffy Antigen Receptor for Chemokines (DARC) gene, CD8+ T-cell density and Aggressive Breast Cancer Subtypes in Black Women.\",\"authors\":\"Nisha M Nair, Lucas Mendicino, Peter N Fiorica, Angela R Omilian, Thaer Khoury, Wiam Bshara, Elisa V Bandera, Chi-Chen Hong, Yara Abdou, Jo L Freudenheim, Anselm J M Hennis, Katie M O'Brien, Gary R Zirpoli, Ebonee N Butler, John Oladapo Obafunwa, Clarice R Weinberg, Dezheng Huo, Bingshan Li, Xingyi Guo, Julie R Palmer, Christopher A Haiman, Wei Zheng, Song Yao, Christine B Ambrosone\",\"doi\":\"10.1158/1055-9965.EPI-25-0454\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Immune response in blood varies by ancestry, linked to an African-specific variant (rs2814778) in DARC/ACKR1. We examined associations between rs2814778, CD8+ T cell density in breast tumors, and breast cancer risk in African-American/Black women.</p><p><strong>Methods: </strong>CD8+ T-cell density in tumors from 428 Black women were examined in relation to the rs2814778 variant. In the African Ancestry Breast Cancer Genetics Consortium (AABCG) with 16,886 cases and 18,044 controls, rs2814778 was evaluated in relation to risk of overall breast cancer and to more aggressive subtypes (ER- and TNBC).</p><p><strong>Results: </strong>Women with the African-specific CC genotype had lower tumor CD8+ T-cell density (87.0 per mm2) than those with TT genotypes (146.6 per mm2; p< 0.05). Each T allele was significantly associated with an increase in T-cell density (p=0.04). In the largest analysis, to date, there were no associations between rs2814778 and risk of overall breast cancer [OR=0.90 (95% CI 0.66-1.22)], or with ER- [OR=0.86 (95% CI 0.68-1.08)] or TNBC [OR=0.77 (95% CI 0.56-1.05)].</p><p><strong>Conclusions: </strong>Although breast tumors from women with the African-specific DARC C allele had lower CD8+ T-cell density levels than those with T alleles, in a large breast cancer consortium with adequate statistical power, the variant was not associated with breast cancer risk overall, nor with risk of ER- or TNBC as previously hypothesized.</p><p><strong>Impact: </strong>Although the 'Duffy-null' allele has been the focus of research as a contributor to aggressive breast cancer in Black women, this study with 34,930 cases and controls found no associations with risk.</p>\",\"PeriodicalId\":520580,\"journal\":{\"name\":\"Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1158/1055-9965.EPI-25-0454\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1055-9965.EPI-25-0454","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:血液中的免疫反应因血统而异,与DARC/ACKR1的非洲特异性变异(rs2814778)有关。我们研究了非裔美国人/黑人女性乳腺肿瘤中rs2814778、CD8+ T细胞密度与乳腺癌风险之间的关系。方法:检测428例黑人女性肿瘤中CD8+ t细胞密度与rs2814778变异的关系。在非洲血统乳腺癌遗传联盟(AABCG)中,有16,886例病例和18,044例对照,rs2814778与总体乳腺癌风险和更具侵袭性的亚型(ER-和TNBC)相关。结果:非洲特异性CC基因型女性的肿瘤CD8+ t细胞密度(87.0 / mm2)低于TT基因型女性(146.6 / mm2;p < 0.05)。每个T等位基因与T细胞密度增加显著相关(p=0.04)。在迄今为止最大规模的分析中,rs2814778与总体乳腺癌风险[OR=0.90 (95% CI 0.66-1.22)]、ER- [OR=0.86 (95% CI 0.68-1.08)]或TNBC [OR=0.77 (95% CI 0.56-1.05)]之间没有关联。结论:尽管来自具有非洲特异性DARC等位基因的女性乳腺癌肿瘤的CD8+ T细胞密度水平低于具有T等位基因的女性,但在具有足够统计能力的大型乳腺癌联盟中,该变异与乳腺癌总体风险无关,也与先前假设的ER-或TNBC风险无关。影响:虽然“Duffy-null”等位基因一直是研究的焦点,因为它是黑人女性侵袭性乳腺癌的一个因素,但这项对34,930例病例和对照组的研究没有发现与风险相关。
The African-specific variant in the Duffy Antigen Receptor for Chemokines (DARC) gene, CD8+ T-cell density and Aggressive Breast Cancer Subtypes in Black Women.
Background: Immune response in blood varies by ancestry, linked to an African-specific variant (rs2814778) in DARC/ACKR1. We examined associations between rs2814778, CD8+ T cell density in breast tumors, and breast cancer risk in African-American/Black women.
Methods: CD8+ T-cell density in tumors from 428 Black women were examined in relation to the rs2814778 variant. In the African Ancestry Breast Cancer Genetics Consortium (AABCG) with 16,886 cases and 18,044 controls, rs2814778 was evaluated in relation to risk of overall breast cancer and to more aggressive subtypes (ER- and TNBC).
Results: Women with the African-specific CC genotype had lower tumor CD8+ T-cell density (87.0 per mm2) than those with TT genotypes (146.6 per mm2; p< 0.05). Each T allele was significantly associated with an increase in T-cell density (p=0.04). In the largest analysis, to date, there were no associations between rs2814778 and risk of overall breast cancer [OR=0.90 (95% CI 0.66-1.22)], or with ER- [OR=0.86 (95% CI 0.68-1.08)] or TNBC [OR=0.77 (95% CI 0.56-1.05)].
Conclusions: Although breast tumors from women with the African-specific DARC C allele had lower CD8+ T-cell density levels than those with T alleles, in a large breast cancer consortium with adequate statistical power, the variant was not associated with breast cancer risk overall, nor with risk of ER- or TNBC as previously hypothesized.
Impact: Although the 'Duffy-null' allele has been the focus of research as a contributor to aggressive breast cancer in Black women, this study with 34,930 cases and controls found no associations with risk.